About this trial
Multicentric, exploratory, non-pharmacologic, retrospective/prospective, translational study aiming to identify the molecular, cellular and psychological-sociological variables predictive of response to chemotherapy in gastric cancer patients.
Eligibility criteria
Qualifiers
Patients with diagnosis of histologically confirmed, potentially resectable adenocarcinoma of the stomach (GC) or the gastric-esophageal junction (GEJ) treated with the standard regimens (5-Fluoro-Uracil or Capecitabine + Oxaliplatin +/- Docetaxel)
Participant is willing and able to give informed consent for participation in the study (prospective and retrospective cohort) or Substitutive Informed Consent Declaration Form will be subscribed by the PI for patients that are not reachable
Male or Female, aged >18 years
Availability of tissue samples and clinico-pathological data for retrospective cohort
Disqualifiers
Age < 18 years
Early Gastric Cancer and T2 (if N0)
Linitis plastica
Positive peritoneal cytology or peritoneal involvement
Trial design
Treatments tested in this trial
- Not listed
Trial groups
Sponsors and collaborators
Istituto Romagnolo per lo Studio dei Tumori Dino Amadori IRST S.r.l. IRCCS
Lead sponsor
ERA PERMED
Collaborator